Ch.10: Molecular structure of chromosomes and transposable elements Flashcards

1
Q

Transposition

A

short segments of DNA, called transposable elements (TEs - Discovered by Barbra McClintock), can move to different sites within chromosome; involves the integration of small segments of DNA
into a new location in the genome

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2
Q

Describe the structure of bacterial chromosomes

A

-Loop domains function to compact the bacterial chromosome
-Bacteria use DNA-binding proteins called nucleoid-associated proteins (NAPs) to form microdomains and macrodomain
- Microdomains are typically 10,000 bp
-macrodomains that are 800,000 to 1,000,000 bp

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3
Q

What is supercoiling? What is underwinding and overwinding?

A

formation of
additional coils due to twisting forces;
Underwinding: DNA is given a turn that unwinds the helix
and causes fewer turns (negative supercoil)
Overwinding: DNA is given a turn that overwinds the helix
and causes more turns (positive supercoil)

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4
Q

What 2 main topoisomerase enzymes control supercoiling in bacteria?

A

-DNA gyrase ( DNA topoisomerase II)
Introduces negative supercoiling, using energy from ATP, relaxes positive supercoils, untangle intertwined DNA molecules;
Two main classes of drugs inhibit topoisomerase II:
1. Quinolones
2. Coumarins

-DNA topoisomerase I
Relaxes negative supercoil

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5
Q

What is the mechanism of action of DNA gyrase?

A

DNA gyrase binds to DNA, cuts it, ligates the cut DNA back together
in a process that uses two ATPs to introduce two negative supercoils

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6
Q

What are the 3 types f DNA sequences that are required for chromosomal replication and segregation?

A
  • Origins of replication: Each chromosome contains many origins of replication necessary to initiate DNA
    replication that are interspersed about every 100,000 base pairs
  • Centromeres: forms a recognition site for the
    kinetochore proteins; required for chromosome sorting during mitosis and meiosis
  • Telomeres: specialized regions at the ends of chromosomes important in replication and for stability
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7
Q

Sequence complexity can be…?

A

unique or non-repetitive, moderately repetitive
or highly repetitive

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8
Q

Unique/non-repetitive sequences

A

s protein-encoding genes as well as intergenic regions

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9
Q

Moderately repetitive sequences

A

Includes genes for rRNA and histones, sequences that regulate gene expression and translation and
transposable elements

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10
Q

Highly repetitive sequences

A
  • Alu family of transposable elements in humans that are approximately 300 bp long
    -Other highly repetitive sequences are clustered together in tandem arrays
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11
Q

General characteristics and different types of transposons

A
  • All transposons have a terminal direct repeat (DR), which is also called a target-site duplication
  • Insertion elements are characterized by the presence of a terminal inverted repeat
  • Long terminal repeat (LTR) retrotransposons and non-LTR retrotransposons are characterized by the presence of a reverse transcriptase gene
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12
Q

Autonomous vs. non-autonomous transposons

A
  • autonomous elements (complete) contain all of the
    information necessary for transposition or retrotransposition
  • Nonautonomous element lacks a gene such as one that
    encodes transposase or reverse transcriptase
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13
Q

Transposons can…

A

carry extra genes, such as genes that encode antibiotic resistance (horizontal transfer)

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14
Q

LTR retrotransposons vs. non-LTR retrotransposons

A

Both carry a reverse transcriptase that copies the sequence for insertion
somewhere else in the chromosome but
LTR retrotransposons contain a long terminal repeat (LTR) sequence

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15
Q

Insertion elements and transposons vs. retrotransposons

A

-Insertion elements and transposons excise themselves and move to a new location on the chromosome
-Retrotransposons make a copy of themselves and insert the copy into a new location on the chromosome

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16
Q

Some repetitive sequences due to the proliferation of transposons

A

-LINEs (long interspersed elements): Occur at 20,000 to 1,000,000 copies per genome (17% of the human genome)
-SINEs (short interspersed elements): Less than 500 bp in length; The SINE Alu sequence is present at about 1,000,000 copies in human genome (10% of the genome)

17
Q

Describe the structure of eukaryotic chromosomes in nondividing cells

A

compact DNA-protein complex is called chromatin; nucleosome: repeating structural unit within eukaryotic chromatin that is
composed of a double-stranded segment of DNA wrapped around an octamer of histone proteins; A histone octamer is composed of two copies each of four different histone proteins (H1-4, H1 links nucleosomes together and compacts them

18
Q

Korenberg and Null

A

The beads-on-a-string model of nucleosome structure by Kornberg and Marcus Null tested Kornberg’s model where DNase I should preferentially cut DNA in the linker region

19
Q

Who demonstrated the importance of H1 histone in organizing the nucleosome and how?

A

Fritz Thoma- Used chromatography and high salt to remove the H1 histones (less compaction)

19
Q

What do nucleosomes form?

A

a compact structure termed the 30 nm fiber

20
Q

What are the 2 types of heterochromatin?

A

-Constitutive heterochromatin: Regions that are always heterochromatic
Permanently inactive with regard to transcription

-Facultative heterochromatin:
Regions that can interconvert between
euchromatin and heterochromatin

20
Q

Euchromatin

A

Less condensed regions of chromosomes; Transcriptionally active

21
Q

Heterochromatin

A

Tightly compacted regions of chromosomes; Transcriptionally inactive (in general

22
Q

How do Condensin and cohesin promote the compaction of metaphase chromosomes?

A
  • Condensin: Plays a critical role in chromosome condensation
  • Cohesin: Plays a critical role in sister chromatid alignment
    -during Interphase, den II enters the nucleus while hes I is in the cytoplasm